A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587409



Internal ID18539004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21212930..21479947hg38UCSC Ensembl
Innerchr22:21567219..21834236hg19UCSC Ensembl
Innerchr22:19897219..20164236hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38267018
hg19267018
hg18267018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062928
Supporting Variants
Samples
Known GenesHIC2, PI4KAP2, POM121L8P, RIMBP3B, RIMBP3C, TMEM191C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3587409
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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